Shows the first gene, BRD4, involved in the fusion event. The designation (name or number) of the chromosome
or contig
on which the variant appears is shown in GFCHROM.The published symbol for the gene of interest is shown in GFSYM. The description of the type of genomic entity that is represented by the published symbol in GFSYM is shown in GFSYMTYP as GENE WITH PROTEIN PRODUCT. The location within a sequence for the observed value in GFORRES is shown in GFGENLOC.
Row 3:
Shows the second gene, MYO10, involved in the fusion event. The designation (name or number) of the chromosome
or contig
on which the variant appears is shown in GFCHROM.The published symbol for the gene of interest is shown in GFSYM. The description of the type of genomic entity that is represented by the published symbol in GFSYM is shown in GFSYMTYP as GENE WITH PROTEIN PRODUCT. The location within a sequence for the observed value in GFORRES is shown in GFGENLOC.
Row 4:
Shows the characterization or classification of the structural changes to the genes as a consequence of the sequence rearrangement BRD4 and MYO10 genes.
Row 5:
Shows the predicted effect of the sequence rearrangement on the original reading
frame
frames of the BRD4
gene
and MYO10 genes.
Row 6:
Shows the read depth, the total number of times thelocus of the fusion event was sequenced.